K-number	K810480
Device name	SCANLAN SUTURE BOOTS
Applicant	Scanlan Intl., Inc.
Product code	KOC
Device class	Class II
Decision date	Mar 13, 1981
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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SCANLAN SUTURE BOOTS

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